IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-42064-1.html
   My bibliography  Save this article

Wastewater sequencing reveals community and variant dynamics of the collective human virome

Author

Listed:
  • Michael Tisza

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Sara Javornik Cregeen

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Vasanthi Avadhanula

    (Baylor College of Medicine)

  • Ping Zhang

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Tulin Ayvaz

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Karen Feliz

    (Baylor College of Medicine)

  • Kristi L. Hoffman

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Justin R. Clark

    (Baylor College of Medicine
    TAILOR Labs, Baylor College of Medicine)

  • Austen Terwilliger

    (Baylor College of Medicine
    TAILOR Labs, Baylor College of Medicine)

  • Matthew C. Ross

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Juwan Cormier

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Hannah Moreno

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Li Wang

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Katelyn Payne

    (Baylor College of Medicine
    Baylor College of Medicine)

  • David Henke

    (Baylor College of Medicine)

  • Catherine Troisi

    (University of Texas Health Science Center at Houston)

  • Fuqing Wu

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health)

  • Janelle Rios

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI))

  • Jennifer Deegan

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI))

  • Blake Hansen

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health)

  • John Balliew

    (El Paso Water Utility)

  • Anna Gitter

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health)

  • Kehe Zhang

    (University of Texas Health Science Center at Houston
    UTHealth Houston School of Public Health
    UTHealth Houston School of Public Health)

  • Runze Li

    (University of Texas Health Science Center at Houston
    UTHealth Houston School of Public Health
    UTHealth Houston School of Public Health)

  • Cici X. Bauer

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health
    UTHealth Houston School of Public Health)

  • Kristina D. Mena

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health)

  • Pedro A. Piedra

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Joseph F. Petrosino

    (Baylor College of Medicine
    Baylor College of Medicine)

  • Eric Boerwinkle

    (University of Texas Health Science Center at Houston
    Texas Epidemiologic Public Health Institute (TEPHI)
    UTHealth Houston School of Public Health)

  • Anthony W. Maresso

    (Baylor College of Medicine
    TAILOR Labs, Baylor College of Medicine)

Abstract

Wastewater is a discarded human by-product, but its analysis may help us understand the health of populations. Epidemiologists first analyzed wastewater to track outbreaks of poliovirus decades ago, but so-called wastewater-based epidemiology was reinvigorated to monitor SARS-CoV-2 levels while bypassing the difficulties and pit falls of individual testing. Current approaches overlook the activity of most human viruses and preclude a deeper understanding of human virome community dynamics. Here, we conduct a comprehensive sequencing-based analysis of 363 longitudinal wastewater samples from ten distinct sites in two major cities. Critical to detection is the use of a viral probe capture set targeting thousands of viral species or variants. Over 450 distinct pathogenic viruses from 28 viral families are observed, most of which have never been detected in such samples. Sequencing reads of established pathogens and emerging viruses correlate to clinical data sets of SARS-CoV-2, influenza virus, and monkeypox viruses, outlining the public health utility of this approach. Viral communities are tightly organized by space and time. Finally, the most abundant human viruses yield sequence variant information consistent with regional spread and evolution. We reveal the viral landscape of human wastewater and its potential to improve our understanding of outbreaks, transmission, and its effects on overall population health.

Suggested Citation

  • Michael Tisza & Sara Javornik Cregeen & Vasanthi Avadhanula & Ping Zhang & Tulin Ayvaz & Karen Feliz & Kristi L. Hoffman & Justin R. Clark & Austen Terwilliger & Matthew C. Ross & Juwan Cormier & Hann, 2023. "Wastewater sequencing reveals community and variant dynamics of the collective human virome," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42064-1
    DOI: 10.1038/s41467-023-42064-1
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-42064-1
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-42064-1?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Davida S. Smyth & Monica Trujillo & Devon A. Gregory & Kristen Cheung & Anna Gao & Maddie Graham & Yue Guan & Caitlyn Guldenpfennig & Irene Hoxie & Sherin Kannoly & Nanami Kubota & Terri D. Lyddon & M, 2022. "Tracking cryptic SARS-CoV-2 lineages detected in NYC wastewater," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Smruthi Karthikeyan & Joshua I. Levy & Peter Hoff & Greg Humphrey & Amanda Birmingham & Kristen Jepsen & Sawyer Farmer & Helena M. Tubb & Tommy Valles & Caitlin E. Tribelhorn & Rebecca Tsai & Stefan A, 2022. "Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission," Nature, Nature, vol. 609(7925), pages 101-108, September.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Mukhlid Yousif & Said Rachida & Setshaba Taukobong & Nkosenhle Ndlovu & Chinwe Iwu-Jaja & Wayne Howard & Shelina Moonsamy & Nompilo Mhlambi & Sipho Gwala & Joshua I. Levy & Kristian G. Andersen & Cath, 2023. "SARS-CoV-2 genomic surveillance in wastewater as a model for monitoring evolution of endemic viruses," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    2. Yunxi Liu & Nicolae Sapoval & Pilar Gallego-García & Laura Tomás & David Posada & Todd J. Treangen & Lauren B. Stadler, 2024. "Crykey: Rapid identification of SARS-CoV-2 cryptic mutations in wastewater," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Kayla G. Barnes & Joshua I. Levy & Jillian Gauld & Jonathan Rigby & Oscar Kanjerwa & Christopher B. Uzzell & Chisomo Chilupsya & Catherine Anscombe & Christopher Tomkins-Tinch & Omar Mbeti & Edward Ca, 2023. "Utilizing river and wastewater as a SARS-CoV-2 surveillance tool in settings with limited formal sewage systems," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    4. Mitchell D. Ramuta & Christina M. Newman & Savannah F. Brakefield & Miranda R. Stauss & Roger W. Wiseman & Amanda Kita-Yarbro & Eli J. O’Connor & Neeti Dahal & Ailam Lim & Keith P. Poulsen & Nasia Saf, 2022. "SARS-CoV-2 and other respiratory pathogens are detected in continuous air samples from congregate settings," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    5. Sung Hee Ko & Pierce Radecki & Frida Belinky & Jinal N. Bhiman & Susan Meiring & Jackie Kleynhans & Daniel Amoako & Vanessa Guerra Canedo & Margaret Lucas & Dikeledi Kekana & Neil Martinson & Limakats, 2024. "Rapid intra-host diversification and evolution of SARS-CoV-2 in advanced HIV infection," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    6. Denis Mongin & Nils Bürgisser & Gustavo Laurie & Guillaume Schimmel & Diem-Lan Vu & Stephane Cullati & Delphine Sophie Courvoisier, 2023. "Effect of SARS-CoV-2 prior infection and mRNA vaccination on contagiousness and susceptibility to infection," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    7. Nicolae Sapoval & Yunxi Liu & Esther G. Lou & Loren Hopkins & Katherine B. Ensor & Rebecca Schneider & Lauren B. Stadler & Todd J. Treangen, 2023. "Enabling accurate and early detection of recently emerged SARS-CoV-2 variants of concern in wastewater," Nature Communications, Nature, vol. 14(1), pages 1-7, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42064-1. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.